The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness-Reference-Cited by-同舟云学术

The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness

Published:1999-11 Issue:5 Volume:65 Page:1349-1358
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Torroni Antonio,Cruciani Fulvio,Rengo Chiara,Sellitto Daniele,López-Bigas Núria,Rabionet Raquel,Govea Nancy,López de Munain Adolfo,Sarduy Maritza,Romero Lourdes,Villamar Manuela,del Castillo Ignacio,Moreno Felipe,Estivill Xavier,Scozzari Rosaria

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

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4. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 and 14484 mtDNA mutations on an mtDNA lineage;Brown;Am J Hum Genet,1997

5. Hearing loss due to the mitochondrial A1555G mutation in Italian families;Casano;Am J Med Genet,1998

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